Basic information Safety Supplier Related

5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid

Basic information Safety Supplier Related

5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid Basic information

Product Name:
5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid
Synonyms:
  • 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid
  • 3-c]pyridine-2-carboxylic acid
  • 1H-Pyrrolo[2,3-c]pyridine-2-carboxylic acid, 5-chloro-
  • 5-Chloro-6-azaindole-2-carboxylic acid
  • 5-Chloro-1H-pyrrolo[2,3-c]pyridin-2-carboxylic acid
CAS:
800401-68-7
MF:
C8H5ClN2O2
MW:
196.59
Product Categories:
  • CHIRAL CHEMICALS
  • Heterocycle-Pyridine series
Mol File:
800401-68-7.mol
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5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid Chemical Properties

Boiling point:
500.9±45.0 °C(Predicted)
Density 
1.644
refractive index 
1.744
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
3.08±0.30(Predicted)
Appearance
Light yellow to yellow Solid
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Safety Information

HazardClass 
IRRITANT
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5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic acid Usage And Synthesis

Uses

5-Chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylic Acid is a useful reactant for preparation of pyrrolopyridinecarboxylic acid amide as inhibitors of glycogen phosphorylase.

Synthesis

800401-67-6

800401-68-7

GENERAL METHOD: To a stirred solution of ethyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-2-carboxylate (1.3 mmol) in ethanol (12 mL) was added 2 M sodium hydroxide solution (1.7 mmol, 1.1 mL). The reaction mixture was heated to reflux for 1 h (for the synthesis of 5-chloro-6-azaindole-2-carboxylic acid) or 2 h (for the synthesis of other derivatives). After evaporation to remove the solvent, water (10 mL) was added and the pH was adjusted with acetic acid to 4.0. The precipitate was collected by filtration and the resulting solid was dried in a desiccator to give the target product 5-chloro-6-azaindole-2-carboxylic acid.

References

[1] Molecules, 2014, vol. 19, # 9, p. 13342 - 13357
[2] Patent: WO2006/59164, 2006, A2. Location in patent: Page/Page column 20-21
[3] Patent: WO2006/67532, 2006, A1. Location in patent: Page/Page column 19
[4] Patent: WO2005/85245, 2005, A1. Location in patent: Page/Page column 18
[5] Patent: WO2004/104001, 2004, A2. Location in patent: Page 35-36

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